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WO2018170234A1 - Méthodes et compositions pour le traitement du cancer - Google Patents

Méthodes et compositions pour le traitement du cancer Download PDF

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Publication number
WO2018170234A1
WO2018170234A1 PCT/US2018/022593 US2018022593W WO2018170234A1 WO 2018170234 A1 WO2018170234 A1 WO 2018170234A1 US 2018022593 W US2018022593 W US 2018022593W WO 2018170234 A1 WO2018170234 A1 WO 2018170234A1
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Prior art keywords
tumor
agent
ammonia
subject
composition
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PCT/US2018/022593
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English (en)
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Marcia C. Haigis
Jessica SPINELLI
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President And Fellows Of Harvard College
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Publication of WO2018170234A1 publication Critical patent/WO2018170234A1/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/075—Ethers or acetals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents

Definitions

  • compositions and methods of treating or preventing cancer in a subject by administering to the subject a composition comprising an agent (e.g., a small molecule, an ammonia scavenger, a kinase inhibitor, an ammonium protonator, or a synthetic biotic) that decreases the amount of ammonia in the subject (e.g. systemically in the subject in the tumor microenvironment, and/or in a tumor in the subject).
  • an agent e.g., a small molecule, an ammonia scavenger, a kinase inhibitor, an ammonium protonator, or a synthetic biotic
  • determining the progression of cancer e.g., breast cancer
  • a tumor e.g., a breast tumor
  • measuring the amount of ammonia e.g., systemic ammonia, ammonia in the tumor microenvironment, and/or ammonia in a tumor
  • measuring the amount of ammonia in the subject thereby determining a second measurement of systemic ammonia, wherein the cancer and/or tumor has progressed if the second measurement is higher than the first measurement.
  • compositions and methods for treating cancer e.g., breast cancer
  • a tumor e.g., a breast tumor
  • the first agent may be a polypeptide, small molecule, or a polynucleotide (e.g., an inhibitory polynucleotide, such as an shRNA).
  • the second agent may be a polypeptide, small molecule, or a polynucleotide (e.g., an inhibitory polynucleotide, such as an shRNA).
  • the first agent and the second agent are administered at different times (e.g., sequentially). In some embodiments, the first agent and the second agent are administered at the same time.
  • an agent e.g., a small molecule, an ammonium scavenger, a kinase inhibitor, an ammonium protonator, or a synthetic biotic
  • an agent e.g., a small molecule, an ammonia scavenger, a kinase inhibitor, an ammonium protonator, or a synthetic biotic
  • the methods described herein further comprise administering an additional agent (i.e., an immune checkpoint inhibitor or a chemotherapeutic inhibitor).
  • an additional agent i.e., an immune checkpoint inhibitor or a chemotherapeutic inhibitor.
  • chemotherapeutic drug resistance in a subject, comprising administering to the subject (e.g., to the subject systemically or locally to a tumor present in the subject) an agent that reduces the amount of ammonia in the subject and a chemotherapeutic agent.
  • kits for preventing or treating immunotherapeutic drug resistance in a subject comprising administering to the subject (e.g., to the subject systemically, or locally to a tumor present in the subject) an agent that reduces the amount of ammonia in the subject (e.g., systemic ammonia and/or the local level of ammonia in the tumor) and an immunotherapeutic agent.
  • Figure 1 has eight parts, A-H, and shows glutamine-derived ammonia is recycled.
  • Part A shows a schematic of underlying question on ammonia in cancer metabolism.
  • Part B shows RNA levels from The Cancer Genome Atlas of ammonia assimilating enzymes in a panel of cancer subtypes run on the "Normal versus Cancer" analytical tool on Oncomine.org. Fold-change (cancer/normal) for GS (Glutamine Synthetase), GDH
  • RNA levels were assessed.
  • A- Ovarian Serous Cystadenocarcinoma B- Colon Adenocarcinoma, C- Rectal Adenocarcinoma, D- Lobular & Ductal Breast Carcinoma, E- Lung Adenocarcinoma, F- Squamous Lung Cell Carcinoma, G- Endometrial Adenocarcinoma, H- Bladder Urothelial Carcinoma, I- Gastric Adenocarcinoma, J- Glioblastoma, K- Pancreatic Adenocarcinoma, L- Hepatocellular Carcinoma, M- Cutaneous Melanoma.
  • Part C shows heat map of % isotope abundance of metabolites with 15 N-mass shifts in MCF7 and T47D cells after 8 hour treatment with 15 N-(amide)glutamine. 211 metabolites were screened for 15 N-isomeric mass shift using mass spectrometry.
  • Part D shows a schematic of expected and unexpected (in gray) 15 N-isomers after treatment with 15 N-(amide)glutamine.
  • Part E shows isotope abundance of novel 15 N-(amide)glutamine derivatives +/- lwM BPTES in MCF7 and T47D cell lines.
  • Part F shows steady-state metabolite abundance of MCF7 cells treated with luM BPTES in the presence or absence of 0.75mM NH4CI.
  • Glu Glutamate M+l
  • Pro Proline M+l
  • Asp Aspartate M+l
  • Cit Citrulline M+l
  • Asa Arginosuccinate M+l .
  • Part H shows a schematic of ammonia recycling through reductive amination catalyzed by GDH. *P ⁇ 0.05, **P ⁇ 0.01, ***P ⁇ 0.001, and ****P ⁇ 0.0001 by paired Student t test. Error bars represent the SEM.
  • Figure 2 has six parts, A-F, and shows free ammonia is primarily assimilated via GDH to generate glutamate and other amino acids.
  • Part A shows propidium iodide staining of cells treated with a dose of NH 4 C1 for 48 hours.
  • Part B shows heat map of fold-change in steady-state abundance of keto- and amino acids involved in transaminase reactions in T47D cells treated with 0.75mM NH 4 C1.
  • Part C shows a schematic of a transaminase reaction.
  • Part D shows isotope abundance of 15 N-isomers in MCF7 cells after 8 hours of treatment with 0.75mM 15 NH4C1.
  • Part F shows isotope abundance of glutamate (M+l) in MCF7 and T47D cells treated for 8 hours with 0.75mM 15 NH4C1 in control and GDH knockdown cells.
  • Part F shows isotope abundance of 15 N-isomers of metabolites downstream of glutamate treated for 8 hours with 0.75mM 15 NH 4 C1 in control and GDH knockdown cells*P ⁇ 0.05, **P ⁇ 0.01, ***P ⁇ 0.001, and ****P ⁇ 0.0001 by paired Student t test. Error bars represent the SEM.
  • Figure 3 has seven parts, A-G, and shows ammonia stimulates breast cancer growth and proliferation.
  • Part A shows a representative images of 3D culture models of MCF7 and T47D cells treated with 0.5mM NH 4 C1 compared to control conditions.
  • Part D shows representative images of MCF7 and T47D cells in control conditions (daily media change) and conditioned media (media changed every 72 hours). Cells were treated for 8 days.
  • Part E shows ammonia measurement in conditioned media compared to control after 8 days.
  • Part G shows nmoles ammonia secreted per cell in conditioned media of cells harboring stable shRNA-mediated knockdown of GDH or control hairpin. *P ⁇ 0.05, **P ⁇ 0.01, ***P ⁇ 0.001, and ****P ⁇ 0.0001 by paired Student t test. Error bars represent the SEM.
  • Figure 4 has five parts, A-E, and shows systemic and tumor autonomous ammonia metabolism contribute to amino acid synthesis.
  • Part A shows measurement of ammonia in the interstitial fluids of the tumor microenvironment compared to plasma isolated from
  • Part E shows schematic of systemic and tumor autonomous ammonia metabolism. *P ⁇ 0.05, **P ⁇ 0.01, ***P ⁇ 0.001, and ****P ⁇ 0.0001 by paired Student t test. Error bars represent the SEM.
  • Figure 5 has two parts, A-B, and shows ammonia assimilating enzymes in cancer. Part A shows enzymatic reactions of the ammonia assimilating enzymes. Carbamoyl Phosphate Synthetase 1 (CPS1), Glutamate Dehydrogenase (GDH), and Glutamine
  • Figure 6 shows a heatmap of Metabolic Derivatives of 15 N-(amide)-glutamine.
  • Figure 7 has two parts, A-B, and shows metabolic Derivatives of 15 N-(amide)- glutamine in MCF7 and T47D.
  • Part A shows isotope abundance of expected 15 N-isomers after treatment with 15 N-(amide)-glutamine. These metabolites are made in direct, enzymatically catalyzed reactions of glutamine with other metabolites.
  • Part B shows isotope abundance of novel 15 N-isomers after treatment with 15 N-(amide)-glutamine. These metabolites are unexpected because the labeled nitrogen on glutamine is liberated as ammonia prior to their synthesis.
  • Figure 8 has four parts, A-D, and shows characterization of the glutaminase inhibitor BPTES in ER(+) breast cancer cell lines.
  • Part A shows cytotoxicity assay by Propidium Iodide staining of cells treated with a dose of BPTES for 48 hours.
  • Part B shows
  • Part C shows steady-state abundance of glutamate, analyzed by mass spectrometry, in MCF7 and T47D cells treated with 1 uM BPTES.
  • Part D shows isotope abundance of expected 15 N-isomers after treatment with 15 N-(amide)-glutamine and 1 uM BPTES.
  • Figure 9 has three parts, A-C, and shows stoichiometric analysis of ammonia recycling.
  • Part A shows schematic of experiment. MCF7 cells were incubated with 15 N2 13 Cs- glutamine (glutamine (M+7)) for 8 hours. Glutaminolysis was measured by the ion counts of glutamate (M+6), in which five carbons and one nitrogen are labeled. Ammonia recycling was measured by glutamate (M+l), in which a single nitrogen atom on glutamate is labeled. Purple circles indicate 13 C isotopes and yellow circles indicate 15 N isotopes.
  • Part B shows the equation for quantification of total glutamates generated in glutaminolysis.
  • Part C shows the ratio of glutamates generated by glutaminolysis in MCF7 cells.
  • Figure 10 has five parts, A-E, and shows the effect of NH 4 C1 on basal metabolic phenotypes.
  • Part D shows pH measurement of media treated with a dose of NH4C1 (0-50 mM)
  • Figure 11 has four parts, A-D, and shows steady-state profile of ammonia treated cells.
  • Part A shows metabolites that were significantly altered (p ⁇ 0.05) in cells treated with 0.75 mM NH4CI compared to control were analyzed using Metaboanalyst 3.0 pathway analysis.
  • Part C shows relative abundance of nucleotides in cells treated with 0.75 mM NH4CI compared to control
  • N 4
  • Figure 12 shows a heatmap of metabolic derivatives of 15 NH4C1. Percent isotope abundance of 15 N-isomers in the nitrogen scan of T47D and MCF7 cells treated with 0.75 mM 15 NH 4 C1.
  • Figure 13 has six parts, A-F, and shows 15 NH4C1 Tracing in MCF7 and T47D cell lines.
  • Part A shows isotope abundance of 15 N-isomers in T47D cells after 8 hours of treatment with 0.75 mM 15 NH4C1.
  • Part B shows schematic of metabolic pathways by which 15 N-isomers acquire labeling from 15 NH4C1.
  • Figure 14 has two parts, A-B, shows GDH knockdown does not affect 15 N-isomers that derive from GS.
  • Part A shows isotope abundance of 15 N-isomers in T47D and MCF7 cells after 8 hours of treatment with 0.75 mM 15 NH4C1 +/- GDH.
  • Part B shows schematic of GS-derived 15 N-isomers.
  • Figure 15 has three parts, A-C, and shows ammonia accelerates proliferation in 2D and 3D culture.
  • Figure 16 has three parts, A-C, and shows ammonia metabolism and biology in fibroblasts.
  • Part B shows isotope abundance of 15 N-isomers in primary human fibroblasts after 8 hours of treatment with 0.75 mM 15 H4C1.
  • ND 15 N- isomer not detected.
  • Part C shows isotope abundance of 15 N-isomers in primary human fibroblasts after 8 hours of treatment with 2.0 mM 15 N-(amide)-glutamine.
  • ND 15 N-isomer not detected.
  • Figure 17 has three parts, A-C, and shows GDH knockdown does not alter basal growth and proliferation in 3D culture.
  • Part A shows a western blot depicting shRNA- mediated knockdown of glutamate dehydrogenase (GDH) compared to control hairpin in MCF7 cells.
  • Figure 18 has two parts, A-B, shows plasma ammonia measurements in T47D xenograft model.
  • Part B shows ammonia measurement in plasma isolated from mice harboring a subcutaneous tumor >100mm 3 on a time course of a bolus intraperitoneal injection of 9.0mmoles/kg 15 NH4C1.
  • Figure 19 shows heat maps of 15 N-isomers in the tumor, plasma, and liver after 15 NH4C1 Tracing in vivo.
  • Figure 20 shows N-isomers in the tumor, plasma and liver after NH l Tracing in vivo.
  • Figure 21 has two parts, A-B, shows ex vivo tracing in T47D xenograft model.
  • Part A shows isotope abundance of 15 N-isomers isolated from the tumors treated with 0.75 mM 15 H4C1.
  • Part B shows isotope abundance of 15 N-isomers isolated from the tumors treated with 2.0 mM 15 N-(amide)-glutamine.
  • Figure 22 has three parts A-C, and shows inhibition of ammonia assimilation in vivo represses tumor growth.
  • Part A shows a western blot of GDH knockdown in T47D xenograft tumors.
  • Figure 23 has two parts, A -B, and shows ammonia metabolism in primary breast cancer patients.
  • Part A shows measurement of ammonia in the microenvironment of tumor and healthy tissue from estrogen receptor positive breast cancer patients. Concentrations are relative to healthy tissue.
  • Figure 24 has four parts, A-D, and shows synergy between ammonia assimilation and glutaminase inhibition in breast cancer.
  • Part A shows schematic depicting the potential synthetic lethality of glutaminase (GLS) inhibition with ammonia assimilation through GDH. Both pathways converge on glutamate synthesis.
  • Part B shows steady-state metabolite levels of glutamate and downstream metabolites in MCF7 cells with DMSO control, 1 uM BPTES alone, and 1 uM BPTES with 1 mM NH4CI.
  • Part C shows representative images of 3D culture growth of breast cancer cells treated with 1 uM BPTES +/- shRNA-mediated GDH depletion.
  • compositions and methods for treating or preventing cancer in a subject by administering to the subject a composition comprising an agent that decreases the amount of systemic ammonia in the subject and/or decreases the amount of ammonia in a tumor present in the subject.
  • methods for determining the progression of cancer and/or a tumor in a subject comprising measuring the amount of ammonia (e.g., systemic ammonia, ammonia in the tumor microenvironment, and/or ammonia in a tumor) in the subject at different times and comparing the ammonia measurements.
  • ammonia e.g., systemic ammonia, ammonia in the tumor microenvironment, and/or ammonia in a tumor
  • compositions and methods for treating cancer or a tumor in a subject by administering to the subject a first agent that inhibits the expression or activity of glutaminase and a second agent that inhibits the expression or activity of glutamate dehydrogenase.
  • drug resistance e.g., chemotherapeutic and/or immunotherapeutic drug resistance
  • an agent e.g., a small molecule or an ammonium scavenger
  • administering means providing a pharmaceutical agent or composition to a subject, and includes, but is not limited to, administering by a medical professional and self-administering.
  • agenf is used herein to denote a chemical compound, a small molecule, a mixture of chemical compounds and/or a biological macromolecule (such as a nucleic acid, a protein, or a peptide).
  • Agents may be identified as having a particular activity by screening assays described herein below. The activity of such agents may render them suitable as a "therapeutic agent” which is a biologically, physiologically, or pharmacologically active substance (or substances) that acts locally or systemically in a subject.
  • amino acid is intended to embrace all molecules, whether natural or synthetic, which include both an amino functionality and an acid functionality and capable of being included in a polymer of naturally-occurring amino acids.
  • exemplary amino acids include naturally-occurring amino acids; analogs, derivatives and congeners thereof; amino acid analogs having variant side chains; and all stereoisomers of any of any of the foregoing.
  • ammonia and “ammonium” are used interchangeably.
  • ammonia is H3.
  • ammonium is H4+.
  • ammonia and/or ammonium is a mixture of NH3 and H4+.
  • ammonia and/or ammonium is a salt.
  • polynucleotide and “nucleic acid” are used interchangeably. They refer to a polymeric form of nucleotides of any length, either deoxyribonucleotides or
  • Polynucleotides may have any three-dimensional structure, and may perform any function, known or unknown.
  • the following are non- limiting examples of polynucleotides: coding or non-coding regions of a gene or gene fragment, loci (locus) defined from linkage analysis, exons, introns, messenger RNA
  • a polynucleotide may comprise modified nucleotides, such as methylated nucleotides and nucleotide analogs. If present,
  • nucleotide structure may be imparted before or after assembly of the polymer.
  • sequence of nucleotides may be interrupted by non-nucleotide components.
  • a polynucleotide may be further modified, such as by conjugation with a labeling component.
  • recombinant polynucleotide means a polynucleotide of genomic, cDNA, semisynthetic, or synthetic origin which either does not occur in nature or is linked to another polynucleotide in a non-natural arrangement.
  • pharmaceutically-acceptable carrier means a pharmaceutically-acceptable material, composition or vehicle, such as a liquid or solid filler, diluent, excipient, or solvent encapsulating material, involved in carrying or transporting the subject compound from one organ, or portion of the body, to another organ, or portion of the body.
  • a therapeutic that "prevents" a disorder or condition refers to a compound that, when administered to a statistical sample prior to the onset of the disorder or condition, reduces the occurrence of the disorder or condition in the treated sample relative to an untreated control sample, or delays the onset or reduces the severity of one or more symptoms of the disorder or condition relative to the untreated control sample.
  • small molecule is a term of the art and includes molecules that are less than about 1000 molecular weight or less than about 500 molecular weight. In one embodiment, small molecules do not exclusively comprise peptide bonds. In another embodiment, small molecules are not oligomeric.
  • Exemplary small molecule compounds which can be screened for activity include, but are not limited to, peptides, peptidomimetics, nucleic acids, carbohydrates, small organic molecules ⁇ e.g., polyketides) (Cane et al. (1998) Science 282:63), and natural product extract libraries.
  • the compounds are small, organic non-peptidic compounds.
  • a small molecule is not biosynthetic.
  • the term "subject' means a human or non-human animal selected for treatment or therapy.
  • tumor microenvironmenf is an art-recognized term and refers to the cellular environment in which the tumor exists, and includes, for example, interstitial fluids surrounding the tumor, surrounding blood vessels, immune cells, other cells, fibroblasts, signaling molecules, and the extracellular matrix.
  • therapeutically-effective amount and “effective amount' as used herein means the amount of an agent which is effective for producing the desired therapeutic effect in at least a sub-population of cells in a subject at a reasonable benefit/risk ratio applicable to any medical treatment.
  • Treating" a disease in a subject or “treating” a subject having a disease refers to subjecting the subject to a pharmaceutical treatment, e.g., the administration of a drug, such that at least one symptom of the disease is decreased or prevented from worsening.
  • the methods described herein relate, in part, to the novel discovery that cancer cells use the ammonium by-product of glutaminolysis in the production of glutamine and other downstream amino acids, thus promoting cancer cell proliferation.
  • provided herein are methods and compositions to treat or prevent cancer in a subject by administering to the subject a composition comprising at least one agent that decreases the amount of ammonia in the subject.
  • the agent may decrease the amount of ammonia in the subject systemically or locally (e.g., within the tumor or in the tumor microenvironment).
  • methods for treating a tumor in a subject by administering a composition comprising at least one agent that decreases the amount of ammonia in the subject (e.g., decreasing systemic ammonia in the subject and/or decreasing the amount of ammonia in the tumor).
  • compositions disclosed herein may decrease the amount of systemic ammonia in the subject by at least 1%, at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%>, at least 65%>, at least 70%, at least 75 %, at least 80%, at least 85%), at least 90%, at least 95%, or at least 99%.
  • the composition may decrease the amount of ammonia in a tumor present in the subject (e.g., a subject with cancer) by at least 1%, at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75 %, at least 80%, at least 85%, at least 90%, at least 95%), at least 99%, or by 100%.
  • a composition may comprise two or more, three or more, four or more, or five or more agents disclosed herein.
  • the composition may decrease the amount of ammonia in a tumor microenvironment (e.g., in the interstitial fluids in the tumor microenvironment) by at least 1%, at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75 %, at least 80%, at least 85%., at least 90%, at least 95%, at least 99%, or by 100%.
  • a composition may comprise two or more, three or more, four or more, or five or more agents disclosed herein.
  • a composition and/or agent disclosed herein may decrease systemic or local ammonia (e.g., local ammonia in a tumor present in a subject) by, for example, inhibiting ammonia production, inhibiting ammonia recycling in glutaminolysis, or facilitating the removal of ammonia from a subject.
  • the agent may be, for example, a small molecule, a glutamine scavenger, an ammonium scavenger, a kinase inhibitor (e.g., sodium
  • ammonium scavenger may refer to any compound that facilitates the removal of ammonia from a subject (e.g., a subject in need thereof).
  • Ammonium scavengers may be found in U.S. Patent 4,650,587, U.S. Patent No. 4,460,555, and U.S. Patent No. 8,642,012, each of which is hereby incorporated in its entirety.
  • the agent may be a synthetic biotic (e.g., a modified bacteria capable of assimilating ammonia, such as SYNB1020).
  • Exemplary agents include, but are not limited to, sodium phenyl acetate, phenylbutyrate,
  • the agent may be a polypeptide or an inhibitory polynucleotide disclosed herein. Agents disclosed herein may be used alone or in combination.
  • determining the progression of cancer in a subject by measuring the amount of systemic ammonia in the subject, thereby determining a first measurement of ammonia; and, after a period of time, measuring the amount of ammonia in the subject, thereby determining a second measurement of ammonia.
  • the cancer has progressed if the second measurement is higher than the first measurement.
  • the method further comprises measuring the amount of ammonia in the subject to determine a third measurement of ammonia, and cancer is considered to have progressed if the third measurement is higher than the second measurement.
  • measurement of ammonia may be systemic ammonia or local levels of ammonia (e.g., ammonia in the tumor, and/or ammonia in the tumor microenvironment). Also disclosed herein are methods of determining the progression of a tumor (e.g., a tumor present in a subject) by measuring the an amount of ammonia, thereby determining a first measurement of ammonia; and, after a period of time, measuring the amount of ammonia, thereby determining a second measurement of ammonia, wherein the tumor has progressed if the second measurement is higher than the first measurement.
  • a tumor e.g., a tumor present in a subject
  • the method further comprising measuring the amount of ammonia to determine a third measurement of ammonia, wherein the tumor has progressed if the third measurement is higher than the second measurement. In some embodiments, the method further comprising measuring the amount of ammonia to determine a third measurement of ammonia, wherein the tumor has progressed if the third measurement is higher than the second measurement.
  • the measurement of ammonia may be systemic ammonia or local levels of ammonia (e.g., ammonia in the tumor, and/or ammonia in the tumor microenvironment).
  • systemic or local ammonia measurements of systemic or local ammonia. Measurements of systemic ammonia or local ammonia may be taken at regular or sporadic intervals. Systemic or local ammonia in a subject may be measured by any means known in the art. For example, systemic ammonia may be measured by a blood test, wherein blood samples are collected from the subject, mixed, and centrifuged. The plasma is then separated, collected, and, optionally, frozen for later testing.
  • Local ammonia may be measured, for example, by direct sampling of the tumor (e.g., sampling of the interstitial fluids of the tumor microenvironment).
  • the period of time between ammonia measurements may be any period of time, and may depend on the type of cancer or tumor.
  • the period of time may be, for example, 1 day, 3 days, 5 days, one week, two weeks, three weeks, one month, two months, three months, four months, five months, six months, seven months, eight months, nine months, ten months, eleven months, one year, two years, or five years.
  • methods of determining the progression of cancer or a tumor further comprises administering an agent disclosed herein (i.e., an agent that decreases the amount of systemic ammonia, the amount of ammonia in a tumor present in a subject, and/or ammonia in the tumor
  • Glutaminase is an amidohydrolase enzyme that generates glutamate from glutamine.
  • Glutamate dehydrogenase is an enzyme responsible for converting a- ketoglutarate to glutamate.
  • glutamate dehydrogenase recycles ammonia to replenish depleted glutamate pools during glutaminase inhibition.
  • glutaminase and glutamate dehydrogenase generate ammonia and, therefore, inhibition of glutaminase and glutamate dehydrogenase in a subject would lead to a decrease of ammonia in the subject.
  • the glutaminase inhibitor is a small molecule. In some embodiments, the glutaminase inhibitor depletes glutamine pools. In some embodiments, the glutaminase inhibitor is a thiourea derivative product.
  • Exemplary glutaminase inhibitors include, but are not limited to, THDP-17, CB-839, and bis-2-(5-phenylacetamido-l,3,4-thiadiazol-2-yl)ethyl sulfide (BPTES).
  • the glutamate dehydrogenase inhibitor is a small molecule.
  • An exemplary glutamate dehydrogenase inhibitor is epigallocatechin-monogallate (EGCG).
  • the first agent may inhibit the expression and/or activity of glutaminase by at least 1%, at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75 %, at least 80%, at least 85%, at least 90%, at least 95%, at least 99%, or by 100%.
  • the second agent may inhibit the expression and/or activity of glutamate dehydrogenase by at least 1%, at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75 %, at least 80%, at least 85%, at least 90%, at least 95%, at least 99%, or by 100%.
  • the methods described herein further comprise administering an additional agent (i.e., an immune checkpoint inhibitor or a chemotherapeutic inhibitor).
  • an additional agent i.e., an immune checkpoint inhibitor or a chemotherapeutic inhibitor.
  • kits for preventing or treating chemotherapeutic drug resistance in a subject comprising administering to the subject (e.g., to the subject systemically or locally to a tumor present in the subject) an agent disclosed herein (e.g., an agent that reduces the amount of ammonia in the subject) in combination with a tumor present in the subject.
  • an agent disclosed herein e.g., an agent that reduces the amount of ammonia in the subject
  • chemotherapeutic agent The agent disclosed herein and the chemotherapeutic agent may be administered at the same time or at different times.
  • an agent disclosed herein e.g., an agent that reduces the amount of ammonia in the subject
  • the agent disclosed herein and the immunotherapeutic agent may be administered at the same time or at different times.
  • the agents and/or compositions described herein may be administered systemically, intravenously, intramuscularly, orally, or locally (e.g., delivered locally to a tumor).
  • the compositions and/or agents disclosed herein may be delivered by any suitable route of administration, including orally, nasally, as by, for example, a spray, rectally, intravaginal, parenterally, intracisternally and topically, as by powders, ointments or drops, including buccally and sublingually.
  • the agents and/or compositions are delivered generally (e.g., via oral or parenteral administration). In certain other
  • the compositions and/or agents are delivered locally through injection.
  • the therapeutics described herein may be administered through conjunctive therapy.
  • Conjunctive therapy includes sequential, simultaneous and separate, and/or co-administration of the compositions and/or agents in such a way that the therapeutic effects of the first agent administered have not entirely disappeared when the subsequent agent is administered.
  • the additional agent may be co-formulated with the first and/or second agent or be formulated in a separate pharmaceutical composition.
  • the compositions and additional agents are administered at the same time or at different times (e.g., the compositions and additional agents are administered sequentially).
  • agent may refer to any compound that inhibits the expression and/or activity of glutaminase, any compound that inhibits the expression and/or activity of glutamate dehydrogenase, or a compound that otherwise decreases the amount of ammonia in a subject and/or a tumor present in the subject.
  • An agent may be a small molecule, an ammonium scavenger, a kinase inhibitor, an ammonium protonator, a synthetic biotic, a polypeptide, or an inhibitory nucleic acid.
  • agents that decrease the amount of ammonia in a subject or in the tumor of the subject include, but are not limited to, sodium phenylacetate, sodium benzoate, sodium phenylbutyrate, glycerol phenylbutyrate, SY B1020, VS-01, and lactulose.
  • Certain embodiments of the methods and compositions disclosed herein relate to the use of small molecule agents e.g., small molecule agents that inhibit the expression or activity of ammonia, glutaminase, or glutamate dehydrogenase.
  • the small molecule decreases the amount of ammonia in the subject by inhibiting its activity (e.g., by binding to ammonia, inhibiting the production of ammonia, or increasing the elimination of ammonia from a subject.
  • an agent disclosed herein is a polypeptide.
  • the polypeptides can be isolated from cells or tissue sources by an appropriate purification scheme using standard protein purification techniques.
  • polypeptides are produced by recombinant DNA techniques.
  • polypeptides can be chemically synthesized using standard peptide synthesis techniques.
  • polypeptide is a chimeric or fusion polypeptide.
  • a fusion or chimeric polypeptide can be produced by standard recombinant DNA techniques. For example, DNA fragments coding for the different polypeptide sequences are ligated together in-frame in accordance with conventional techniques, for example by employing blunt-ended or stagger- ended termini for ligation, restriction enzyme digestion to provide for appropriate termini, filling-in of cohesive ends as appropriate, alkaline phosphatase treatment to avoid undesirable joining, and enzymatic ligation.
  • the fusion gene can be synthesized by conventional techniques including automated DNA synthesizers.
  • PCR amplification of gene fragments can be carried out using anchor primers which give rise to complementary overhangs between two consecutive gene fragments which can subsequently be annealed and re-amplified to generate a chimeric gene sequence (see, for example, Current Protocols in Molecular Biology, Ausubel et al., eds., John Wiley & Sons: 1992).
  • anchor primers which give rise to complementary overhangs between two consecutive gene fragments which can subsequently be annealed and re-amplified to generate a chimeric gene sequence.
  • polypeptides described herein can be produced in prokaryotic or eukaryotic host cells by expression of polynucleotides encoding a polypeptide(s). Alternatively, such peptides can be synthesized by chemical methods. Methods for expression of heterologous polypeptides in recombinant hosts, chemical synthesis of polypeptides, and in vitro translation are well known in the art and are described further in Maniatis et al., Molecular Cloning: A Laboratory Manual (1989), 2nd Ed., Cold Spring Harbor, N. Y.; Berger and Kimmel, Methods in Enzymology, Volume 152, Guide to Molecular Cloning Techniques (1987), Academic Press, Inc., San Diego, Calif ; Merrifield, J.
  • an agent disclosed herein is an inhibitory polynucleotide.
  • the inhibitory RNA molecules is administered to the subject. Alternatively, constructs encoding these may be contacted with or introduced into the subject.
  • Antisense constructs, antisense oligonucleotides, RNA interference constructs or siRNA duplex RNA molecules can be used to interfere with activity or expression of a target of interest, e.g., glutaminase or glutamate dehydrogenase.
  • Antisense or RNA interference molecules can be delivered in vivo, e.g., injected into tissues of a subject. Typical delivery means known in the art can be used.
  • an interfering RNA can be delivered systemically using, for example, the methods and compositions described in PCT Application No:
  • PCT/US09/036223 PCT/US09/061381 PCT/US09/063927, PCT/US09/063931 and
  • the siRNA is delivered locally.
  • local delivery to the tumor may be accomplished by injection.
  • the interfering RNA described herein when used to cancer, the interfering RNA can be delivered intravenously or parenterally.
  • Actual dosage levels of the agents to be administered may be varied so as to obtain an amount of the active ingredient (e.g., an agent described herein) which is effective to achieve the desired therapeutic response for a particular patient, composition, and mode of administration, without being toxic to the patient.
  • the selected dosage level will depend upon a variety of factors including the activity of the particular agent employed, the route of administration, the time of administration, the rate of excretion or metabolism of the particular compound being employed, the duration of the treatment, other drugs, compounds and/or materials used in combination with the particular compound employed, the age, sex, weight, condition, general health and prior medical history of the patient being treated, and like factors well known in the medical arts.
  • a physician or veterinarian having ordinary skill in the art can readily determine and prescribe the effective amount of the pharmaceutical composition required.
  • the physician or veterinarian could prescribe and/or administer doses of the compounds employed in the pharmaceutical composition at levels lower than that required in order to achieve the desired therapeutic effect and gradually increase the dosage until the desired effect is achieved.
  • compositions e.g., pharmaceutical compositions, containing at least one agent (e.g., an agent that inhibits the expression and/or activity of glutaminase, an agent that inhibits the expression and/or activity of glutamate dehydrogenase, or a compound that otherwise decreases the amount of ammonia in a subject and/or a tumor) described herein together with a pharmaceutically acceptable carrier.
  • the composition includes a combination of multiple (e.g., two or more) agents described herein.
  • compositions that comprise an agent (e.g., a small molecule or an ammonium scavenger) that decreases the amount of ammonia in the subject.
  • agent e.g., a small molecule or an ammonium scavenger
  • the agent may decrease ammonia in the subject by decreasing ammonia production, decreasing ammonia recycling, or increasing ammonia excretion.
  • compositions comprising at a first agent (e.g., a small molecule, a polypeptide, an inhibitory nucleic acid) that inhibits the expression or activity of glutaminase and a second agent (e.g., a small molecule, a polypeptide, or an inhibitory nucleic acid) that inhibits the expression or activity of glutamate dehydrogenase described herein together with a pharmaceutically acceptable carrier.
  • a first agent e.g., a small molecule, a polypeptide, an inhibitory nucleic acid
  • a second agent e.g., a small molecule, a polypeptide, or an inhibitory nucleic acid
  • the compositions include a combination of multiple (e.g., three or more) agents described herein.
  • the first agent may be a polypeptide, small molecule, or an inhibitory polynucleotide.
  • the second agent may be a polypeptide, small molecule, or an inhibitory polynucleotide.
  • the agents and/or compositions are delivered locally.
  • the agents and/or compositions e.g., pharmaceutical compositions
  • the agent or pharmaceutical composition is administered with an additional therapeutic agent.
  • the additional therapeutic agent is a chemotherapeutic agent.
  • chemotherapeutic agents include alkylating agents such as thiotepa and cyclophosphamide (CytoxanTM); alkyl sulfonates such as busulfan, improsulfan and piposulfan; aziridines such as benzodopa, carboquone, meturedopa, and uredopa; emylerumines and memylamelamines including alfretamine, triemylenemelamine, triethylenephosphoramide, triethylenethiophosphoramide, and trimemylolomelamine; acetogenins (especially bullatacin and bullatacinone); a camptothecin (including synthetic analogue topotecan); bryostatin; cally statin; CC-1065 (including its adozelesin, carzelesin and bizelesin synthetic analogues); cryptophycins (articularly cryptophycin 1 and cryptophycin 8); dolastatin;
  • spongistatin nitrogen mustards such as chlorambucil, chlornaphazine, cholophosphamide, estramustine, ifosfamide, mechlorethamine, mechlorethamine oxide hydrochloride, melphalan, novembichin, phenesterine, prednimustine, trofosfamide, uracil mustard;
  • nitrogen mustards such as chlorambucil, chlornaphazine, cholophosphamide, estramustine, ifosfamide, mechlorethamine, mechlorethamine oxide hydrochloride, melphalan, novembichin, phenesterine, prednimustine, trofosfamide, uracil mustard;
  • nitrosoureas such as carmustine, chlorozotocin, foremustine, lomustine, nimustine, ranimustine; antibiotics such as the enediyne antibiotics (e.g., calicheamicin, especially calicheamicin gammall and calicheamicin phili); dynemicin, including dynemicin A;
  • bisphosphonates such as clodronate; an esperamicin; as well as neocarzinostatin
  • aclacinomysins actinomycin, authramycin, azaserine, bleomycins, cactinomycin, carabicin, carrninomycin, carzinophilin, chromomycins, dactinomycin, daunorubicin, detorubicin, 6- diazo-5-oxo-L-norleucine, doxorubicin (AdramycinTM) (including morpholino-doxorubicin, cyanomorpholino-doxorubicin, 2-pyrrolino-doxorubicin and deoxydoxorubicin), epirubicin, esorubicin, idarubicin, marcellomycin, mitomycins such as mitomycin C, mycophenolic acid, nogalamycin, olivomycins, peplomycin, potfiromycin, puromycin, quelamycin, rodorubicin, streptonigrin, streptozocin, tubercidin, ubenimex
  • aminolevulinic acid aminolevulinic acid
  • eniluracil amsacrine; hestrabucil; bisantrene; edatraxate; defofamine; demecolcine; diaziquone; elformthine; elliptinium acetate; an epothilone; etoglucid; gallium nitrate; hydroxyurea; lentinan; lonidamine; maytansinoids such as maytansine and ansamitocins; mitoguazone; mitoxantrone; mopidamol; nitracrine; pentostatin; phenamet; pirarubicin; losoxantrone; podophyllinic acid; 2-ethylhydrazide; procarbazine; PSKTM;
  • razoxane rhizoxin; sizofiran; spirogermanium; tenuazonic acid; triaziquone; 2,2',2"- tricUorotriemylamine; trichothecenes (especially T-2 toxin, verracurin A, roridin A and anguidine); urethane; vindesine; dacarbazine; mannomustine; mitobronitol; mitolactol;
  • paclitaxel TexolTM, Bristol Meyers Squibb Oncology, Princeton, N.J.
  • docetaxel TaxoteretTM, Rhone-Poulenc Rorer, Antony, France
  • chlorambucil gemcitabine
  • mitroxantrone vancristine; vinorelbine (NavelbineTM); novantrone; teniposide; edatrexate; daunomycin; aminopterin; xeoloda; ibandronate; CPT-11; topoisomerase inhibitor RFS 2000; difluoromethylornithine (DMFO); retinoids such as retinoic acid; capecitabine; and pharmaceutically acceptable salts, acids or derivatives of any of the above.
  • DMFO difluoromethylornithine
  • chemotherapeutic agent anti-hormonal agents that act to regulate or inhibit hormone action on tumors
  • anti-estrogens and selective estrogen receptor modulators SERMs
  • SERMs selective estrogen receptor modulators
  • tamoxifen including NolvadexTM
  • raloxifene including NolvadexTM
  • droloxifene 4-hydroxytamoxifen
  • trioxifene keoxifene
  • LY117018 4-hydroxytamoxifen
  • toremifene FarestonTM
  • inhibitors of the enzyme aromatase which regulates estrogen production in the adrenal glands, such as, for example, 4(5)-imidazoles, aminoglutethimide, megestrol acetate (MegaceTM), exemestane, formestane, fadrozole, vorozole (RivisorTM), letrozole (FemaraTM), and anastrozole (ArimidexTM)
  • anti-androgens such as flutamide
  • the additional therapeutic agent is an immune checkpoint inhibitor.
  • Immune Checkpoint inhibition broadly refers to inhibiting the checkpoints that cancer cells can produce to prevent or downregulate an immune response.
  • immune checkpoint proteins are CTLA-4, PD-1, VISTA, B7-H2, B7-H3, PD-L1, B7-H4, B7-H6, ICOS, HVEM, PD-L2, CD160, gp49B, PIR-B, KIR family receptors, TIM-1, TIM-3, TIM-4, LAG-3, BTLA, SIRPalpha (CD47), CD48, 2B4 (CD244), B7.1, B7.2, ILT-2, ILT-4, TIGIT, HHLA2, butyrophilins, A2aR, and combinations thereof.
  • compositions and/or agents disclosed herein may be specially formulated for administration in solid or liquid form, including those adapted for the following: (1) oral administration, for example, drenches (aqueous or non-aqueous solutions or suspensions), tablets, e.g., those targeted for buccal, sublingual, and systemic absorption, boluses, powders, granules, pastes for application to the tongue; or (2) parenteral administration, for example, by subcutaneous, intramuscular, intravenous, intrathecal, intracerebral or epidural injection as, for example, a sterile solution or suspension, or sustained-release formulation.
  • oral administration for example, drenches (aqueous or non-aqueous solutions or suspensions), tablets, e.g., those targeted for buccal, sublingual, and systemic absorption, boluses, powders, granules, pastes for application to the tongue
  • parenteral administration for example, by subcutaneous, intramuscular, intravenous, intrathecal, intracer
  • Methods of preparing pharmaceutical formulations or compositions include the step of bringing into association an agent described herein with the carrier and, optionally, one or more accessory ingredients.
  • the formulations are prepared by uniformly and intimately bringing into association an agent described herein with liquid carriers, or finely divided solid carriers, or both, and then, if necessary, shaping the product.
  • compositions suitable for parenteral administration comprise one or more agents described herein in combination with one or more pharmaceutically-acceptable sterile isotonic aqueous or non-aqueous solutions, dispersions, suspensions or emulsions, or sterile powders which may be reconstituted into sterile injectable solutions or dispersions just prior to use, which may contain sugars, alcohols, antioxidants, buffers, bacteriostats, solutes which render the formulation isotonic with the blood of the intended recipient or suspending or thickening agents.
  • aqueous and non-aqueous carriers examples include water, ethanol, dimethyl sulfoxide (DMSO), polyols (such as glycerol, propylene glycol, polyethylene glycol, and the like), and suitable mixtures thereof, vegetable oils, such as olive oil, and injectable organic esters, such as ethyl oleate.
  • DMSO dimethyl sulfoxide
  • polyols such as glycerol, propylene glycol, polyethylene glycol, and the like
  • vegetable oils such as olive oil
  • injectable organic esters such as ethyl oleate.
  • Proper fluidity can be maintained, for example, by the use of coating materials, such as lecithin, by the maintenance of the required particle size in the case of dispersions, and by the use of surfactants.
  • kits for treating a cancer by administering to a subject (e.g., to a tumor present in a subject) a composition comprising an agent described herein.
  • the methods described herein may be used to treat any cancerous or pre-cancerous tumor.
  • the cancer includes a solid tumor.
  • Cancers that may be treated by methods and compositions provided herein include, but are not limited to, cancer cells from the bladder, blood, bone, bone marrow, brain, breast (e.g., estrogen receptor (ER)-positive breast cancer, triple negative breast cancer, or HER2 positive breast cancer), colon, esophagus, gastrointestine, gum, head, kidney, liver, lung,
  • ER estrogen receptor
  • the cancer may specifically be of the following histological type, though it is not limited to these: neoplasm, malignant; carcinoma; carcinoma, undifferentiated; giant and spindle cell carcinoma; small cell carcinoma; papillary carcinoma; squamous cell carcinoma;
  • lymphoepithelial carcinoma basal cell carcinoma; pilomatrix carcinoma; transitional cell carcinoma; papillary transitional cell carcinoma; adenocarcinoma; gastrinoma, malignant; cholangiocarcinoma; hepatocellular carcinoma; combined hepatocellular carcinoma and cholangiocarcinoma; trabecular adenocarcinoma; adenoid cystic carcinoma; adenocarcinoma in adenomatous polyp; adenocarcinoma, familial polyposis coli; solid carcinoma; carcinoid tumor, malignant; branchiolo-alveolar adenocarcinoma; papillary adenocarcinoma;
  • chromophobe carcinoma acidophil carcinoma; oxyphilic adenocarcinoma; basophil carcinoma; clear cell adenocarcinoma; granular cell carcinoma; follicular adenocarcinoma; papillary and follicular adenocarcinoma; nonencapsulating sclerosing carcinoma; adrenal cortical carcinoma; endometrioid carcinoma; skin appendage carcinoma; apocrine adenocarcinoma; sebaceous adenocarcinoma; ceruminous adenocarcinoma; mucoepidermoid carcinoma; cystadenocarcinoma; papillary cystadenocarcinoma; papillary serous
  • cystadenocarcinoma mucinous cystadenocarcinoma; mucinous adenocarcinoma; signet ring cell carcinoma; infiltrating duct carcinoma; medullary carcinoma; lobular carcinoma;
  • inflammatory carcinoma mammary paget's disease; acinar cell carcinoma; adenosquamous carcinoma; adenocarcinoma w/squamous metaplasia; malignant thymoma; malignant ovarian stromal tumor; malignant thecoma; malignant granulosa cell tumor; and malignant roblastoma; Sertoli cell carcinoma; malignant leydig cell tumor; malignant lipid cell tumor; malignant paraganglioma; malignant extra-mammary paraganglioma; pheochromocytoma; glomangiosarcoma; malignant melanoma; amelanotic melanoma; superficial spreading melanoma; malignant melanoma in giant pigmented nevus; epithelioid cell melanoma;
  • myxosarcoma liposarcoma; leiomyosarcoma; rhabdomyosarcoma; embryonal
  • rhabdomyosarcoma alveolar rhabdomyosarcoma; stromal sarcoma; malignant mixed tumor; mullerian mixed tumor; nephroblastoma; hepatoblastoma; carcinosarcoma; malignant mesenchymoma; malignant brenner tumor; malignant phyllodes tumor; synovial sarcoma; malignant mesothelioma; dysgerminoma; embryonal carcinoma; malignant teratoma;
  • lymphangiosarcoma osteosarcoma; juxtacortical osteosarcoma; chondrosarcoma; malignant chondroblastoma; mesenchymal chondrosarcoma; giant cell tumor of bone; ewing's sarcoma; malignant odontogenic tumor; ameloblastic odontosarcoma; malignant ameloblastoma;
  • ameloblastic fibrosarcoma malignant pinealoma; chordoma; malignant glioma;
  • ependymoma ependymoma; astrocytoma; protoplasmic astrocytoma; fibrillary astrocytoma; astroblastoma; glioblastoma; oligodendroglioma; oligodendroblastoma; primitive neuroectodermal;
  • cerebellar sarcoma cerebellar sarcoma; ganglion euroblastoma; neuroblastoma; retinoblastoma; olfactory neurogenic tumor; malignant meningioma; neurofibrosarcoma; malignant neurilemmoma; malignant granular cell tumor; malignant lymphoma; Hodgkin's disease; Hodgkin's lymphoma; paragranuloma; small lymphocytic malignant lymphoma; diffuse large cell malignant lymphoma; follicular malignant lymphoma; mycosis fungoides; other specified non-Hodgkin's lymphomas; malignant histiocytosis; multiple myeloma; mast cell sarcoma; immunoproliferative small intestinal disease; leukemia; lymphoid leukemia; plasma cell leukemia; erythroleukemia; lymphosarcoma cell leukemia; myeloid leukemia; basophil
  • the subject has cancer (e.g., breast cancer, such as ER-positive breast cancer).
  • the cancer comprises a solid tumor.
  • the tumor is an adenocarcinoma, an adrenal tumor, an anal tumor, a bile duct tumor, a bladder tumor, a bone tumor, a blood born tumor, a brain/CNS tumor, a breast tumor, a cervical tumor, a colorectal tumor, an endometrial tumor, an esophageal tumor, an Ewing tumor, an eye tumor, a gallbladder tumor, a gastrointestinal, a kidney tumor, a laryngeal or hypopharyngreal tumor, a liver tumor, a lung tumor, a mesothelioma tumor, a multiple myeloma tumor, a muscle tumor, a nasopharyngeal tumor, a neuroblastoma, an oral tumor, an osteosarcoma, an ovarian tumor, a pan
  • Ammonia is a ubiquitous byproduct of cancer metabolism, however its fate has remained elusive. Here it is identified that ammonia is not merely a toxic waste product of cancers, but is recycled into central amino acid metabolism to maximize nitrogen utilization. Cancer cells primarily assimilate ammonia via reductive amination catalyzed by glutamate dehydrogenase (GDH), and secondary reactions enable other amino acids, such as proline and aspartate, to directly acquire this nitrogen. It was discovered that metabolic recycling of ammonia fosters accelerated breast cancer proliferation in 2D and 3D breast cancer culture models. In vivo, ammonia accumulates in the tumor microenvironment, and can be directly utilized to generate amino acids. Taken together, these data reorient the dogma that ammonia is a secreted waste product and for the first time highlights its role as a
  • Glutamine is considered the "nitrogen reservoir" for cancer cells due to its anabolic role in nucleotide production.
  • the role of glutamine as a nitrogen reservoir is contradicted in catabolic glutamine metabolism, since nitrogen is liberated as the by-product ammonia.
  • the fate of ammonia in tumor metabolism has never been determined. It was hypothesized that this ammonia may be re-assimilated into central metabolism to maximize the efficiency of nitrogen utilization. In this study, it was sought to elucidate the fate of ammonia in cancer as 1) a toxic waste product or 2) a biosynthetic metabolite ( Figure 1, Part A).
  • CPS1 carbamoyl phosphate synthetase I
  • GDH glutamate dehydrogenase
  • GS glutamine synthetase
  • FIG. 5 Part A Bioinformatic analysis of patient data from The Cancer Genome Atlas of RNA levels for the ammonia assimilating enzymes in healthy compared to cancerous tissues revealed that GS and GDH expression were significantly increased across multiple cancer subtypes ( Figure 2, Part B & Figure 5, Part B). Moreover, CPS1, which is normally expressed in the liver, was not induced in many cancer subtypes. Of note, breast cancers displayed increased expression of both GS and GDH compared to healthy breast tissue. Specifically, ER positive breast cancers induced GS and GDH compared to other subtypes. Therefore, ER positive breast cancer was used as a representative model to probe for ammonia assimilation.
  • a metabolic tracing analysis was performed using a targeted hydrophilic interaction liquid chromatography coupled to mass spectrometry (HILIC-MS) method and assessed the fate of 15 N(amide)-glutamine, which liberates 15 H 3 via glutaminase activity.
  • HILIC-MS hydrophilic interaction liquid chromatography coupled to mass spectrometry
  • M+l indicates a single 15 N-mass shift
  • M+2 indicates two 15 N-mass shifts
  • M+3 indicates three 15 N-mass shifts
  • M+4 indicates four 15 N-mass shifts
  • M+5 indicates five 15 N-mass shifts
  • M+6 indicates six 15 N-mass shifts
  • M+7 indicates seven 15 N-mass shifts.
  • GDH-catalyzed reductive amination is prevalent in the liver, where there is a sufficient concentration of ammonia to enable this direction of catalytic activity. It was postulated that elevated levels of ammonia in the tumor microenvironment may likewise be permissive of GDH-catalyzed reductive amination.
  • NH l ammonium chloride
  • Physiological concentrations of ammonia range between 0-50 ⁇ in healthy adults, 50-150 ⁇ in newborns, and up to l .OmM in patients with hyperammonemia.
  • Supraphysiological levels of ammonia are toxic to neurons, fueling the dogma that ammonia may also be toxic to tumor cells.
  • NH 4 C1 was not cytotoxic to tumor cells even at a concentration of 50 mM, contrasting the toxicity of ammonia reported for neurons ( Figure 2, Part A). Moreover, ammonia concentrations of 0- 10 mM did not alter glucose and glutamine uptake, or basal respiration ( Figure 10, Parts A- C). In addition, ammonia did not alter pH of media ( Figure 10, Part D).
  • ammonium NH4 +
  • NH3 ammonia
  • Ammonia assimilation in yeast has a fundamental role in supporting growth and proliferation. As ammonia was not toxic to tumor cells, it was tested whether ammonia facilitates breast cancer growth and proliferation (Figure 2, Part A). As in yeast, addition of physiological levels of ammonia supported increased proliferation in a panel of breast cancer cell lines ( Figure 15, Parts A-B). Moreover, in 3D culture, ammonia stimulates sphere growth and cell proliferation ( Figure 3, Parts A-B & Figure 14, Part C). Contrary to breast cancer cells, proliferation in primary human fibroblasts was not changed by ammonia (Figure 16, Part A). Using 15 NH 4 C1 tracing, it was found that fibroblasts centrally assimilated ammonia to generate glutamine (Figure 16, Part B).
  • glutamine and glutamate labeling in the tumor. Since labeled glutamine and glutamate are also found in the liver and plasma, it is indistinguishable whether these 15 N-isomers can be generated in a tumor autonomous manner. Furthermore, the kinetics of glutamine labeling in the tumor implies that a subset of the labeled glutamine pool in the tumor may be taken up from the plasma.
  • ammonia is not simply a metabolic waste product, and is recycled to support the high demand for amino acid synthesis in rapidly proliferating cells.
  • ammonia is often considered a toxin, herein it is shown that it stimulates growth and proliferation in breast cancer. This stimulatory effect is directly mediated by GDH-catalyzed ammonia assimilation.
  • ammonia accumulates in the tumor microenvironment, and is utilized by cancer cells for amino acid synthesis in vivo. These biosynthetic pathways are supported in both systemic and tumor autonomous metabolism.
  • 2D cell culture All breast cancer cell lines were cultured in Glutamine-Free RPMI (Life Technologies) supplemented with 5% FBS (Life Technologies) and 1% Penicillin and Streptomycin (Invitrogen). 2 mM L-Glutamine (Sigma) was added to the media on the day of the experiment to minimize glutamine degradation and subsequent ammonium
  • 3D cell culture MCF7 and T47D cells that have been adapted to culture conditions for four days were incubated in 8-well glass chamber culture slides (BD Falcon) on a bed of LDEV-free MatriGel (Corning) in RPMI supplemented with 5% FBS, 1%
  • Penicillin/Streptomycin and 2% MatriGel Two days after seeding cells, media was replaced in all conditions. For control and ammonium-treated conditions media was changed daily for the duration of the experiment. For studies on conditioned media, media was changed every three days. Images were taken on a Nikon Eclipse TE2000-U Microscope after 8 days or 11 days for MCF7 and T47D cells, respectively. Sphere area was quantified using ImageJ on 200-300 colonies per replicate. Cells were harvested after incubation in Cell Recovery Solution (Corning: 354253) for one hour at 4°C and counted with a Beckman Coulter Counter.
  • Proliferation Assays Cell lines were adapted to medium conditions containing 0.0 mM, 0.1 mM, or 0.5 mM NFLCl for four days prior to experimentation. 25,000 cells were seeded in triplicate in 6-well dishes and counted daily for approximately one week on a
  • Oncomine Database Analysis Patient data from The Cancer Genome Atlas (TCGA) was analyzed using the 'Cancer Versus Normal' analytical tool on the public database Oncomine. Datasets were filtered for a threshold P-value ⁇ 0.0001 and assessed for both Over-expression Fold-Change and Under-expression Fold-Change in mRNA levels relative to healthy tissue as measured with a Human Genome U133A Array.
  • Antibody (1 :5000, Cell Signaling), Anti-mouse IgG FIRP-linked Antibody (1 :5000, Cell
  • Blots were developed using Pierce ECL Western Blotting Substrate (Thermo).
  • shRNAs against GDH1/2 were subcloned into the pLKO. l puro vector (Addgene Plasmid #8453) at EcoRI and Agel sites: shControl:
  • Subcloned plasmids were transfected into HEK293T cells. MCF7 and T47D cells were subsequently infected with the lentivirus, generating stable GDH knockdown cell lines.
  • Glutamine and Ammonia Tracing Prior to experimentation, cells were adapted to respective media conditions for four days. Following adaptation, cells were seeded in 6-cm plates as previously described. After 24 hours media was replaced with RPMI supplemented with 2 mM L-Glutamine (amide- 15 N) (Sigma, 98% isotopic purity), or 2 mM L-Glutamine ( 13 Cs, 15 N2) (Sigma, 98% isotopic purity), or 0.75 mM 15 H4C1 (Sigma, 98% isotopic purity). Cells were incubated with metabolic isotopes for on a time course (0-12 hours) or for 8 hours and polar metabolites were extracted as previously described.
  • Mass Spectrometry Metabolites were isolated in 80% MeOH and analyzed on two distinct methods of hydrophilic interaction liquid chromatography coupled to mass spectrometry (HILIC-MS). In one method, electrospray ionization was tailored to negative- ion mode, and in the second method to positive-ion mode. For negative-ion mode, analytes were eluted in Buffer A (20 mM Ammonium Acetate, 20 mM Ammonium Hydroxide) and Buffer B (10 mM Ammonium Hydroxide in 75:25 Acetonitrile:Methanol).
  • Buffer A (20 mM Ammonium Acetate, 20 mM Ammonium Hydroxide
  • Buffer B 10 mM Ammonium Hydroxide in 75:25 Acetonitrile:Methanol.
  • Samples were run on a HILIC silica (3um, 2.1 x 150mm) column (Waters) with a binary flow rate of 0.4mL/min for 10 minutes on linear gradient (95% Buffer B to 0% Buffer B) followed by 2 minutes with (0% Buffer B) and ending with a 2 minute linear gradient (0% Buffer B to 95% Buffer B) and holding (95% Buffer B) for 13 minutes.
  • samples were dried down and reconstituted in a 20:70: 10: acetonitrile: MeOH: water mixture.
  • the buffers were: Buffer A (10 mM Ammonium Formate, 0.1% formic acid in water) and Buffer B (Acetonitrile, 0.1% formic acid).
  • a master mix of reference standards for metabolites in the targeted method were run immediately prior to each set of samples, such that their retention times were associated with peaks in the unknown samples run over that same column. Peaks were integrated in Tracefinder 3.3.
  • masses for 15 N-isomers were assessed on every targeted metabolite containing nitrogen atom(s).
  • mass spectrum from control samples (not treated with metabolite isotopes) were scanned for the same 15 N-isotopes.
  • Metaboanalyst Pathway Analysis Metabolites were sorted based on their statistical significance (students two-tailed T-Test) on fold-change of relative abundance (normalized peak area) in ammonium-treated cells compared to control. Metabolites altered with the statistical cutoff p ⁇ 0.05 were submitted to MetaboAnalyst 3.0 Pathway Enrichment Analysis Software.
  • Respiration was assessed using the Seahorse XFe-96 Analyzer
  • MCF7 and T47D cells were pre-treated for 1 hour in normal media conditions with a dose of ammonium chloride (0 mM-50 mM). Following this incubation, media was changed to a non-buffered, serum-free Seahorse Media (Seahorse Bioscience, Catalog #102353) supplemented with 5 mM glucose, 2 mM L-glutamine, 1 mM sodium pyruvate, and the appropriate ammonium concentration.
  • Oxygen consumption rate (OCR) was measured over a period of 30 minutes, and values were normalized to cell number.
  • Metabolite Uptake/Secretion Analysis Glucose and glutamine uptake and lactate and ammonium secretion were assessed using the NOVA BioProfile Flex Analyzer (NOVA Biomedical). Control media (no cells) and cells treated with a dose of ammonium chloride (0 mM-50 mM) were incubated for 24 hours and run on the Bioanalyzer. Values for glucose, glutamine, lactate and ammonium in the experimental conditions were subtracted from the values in the respective control media and normalized to cell number.
  • mice All mouse protocols were approved by the Institutional Animal Care and Use Committee (IACUC) at Harvard University. Female athymic nude mice
  • mice harboring subcutaneous tumors that are > 100mm 3 were injected intraperitoneal with a bolus of NH 4 C1 (9.0 mmoles/kg) in two 50 iiL injections.
  • a bolus of NH 4 C1 (9.0 mmoles/kg) in two 50 iiL injections.
  • twelve mice were injected with 15 ⁇ 4 0 in Hanks' Balanced Salt solution (Sigma H6648) and sacrificed 1 hour, 2 hours, and 4 hours post-injection.
  • a control mouse was injected with an equivalent amount of NH4CI and sacrificed two hours after injection, a time determined to be the peak of ammonium levels in plasma after ammonium injection. Livers and tumors were excised, flash-frozen and powderized.
  • Polar metabolites were extracted from 8mg tissue in 80%MeOH and profiled on LC/MS as previously described. Blood was collected from each mouse via heart puncture into heparin tubes and centrifuged at 1500 x g to separate plasma. Metabolites were extracted from plasma in 1 : 10 (v:v) plasma: 80% MeOH and centrifuged at 10,000 x g for 10 minutes at 4°C. Supernatant was run on LC/MS to profile metabolites as previously described.
  • Interstitial fluid from the tumor microenvironment was isolated using a validated protocol (39). Briefly, tumors >100mm 3 were excised, washed with lmL PBS, and blotted dry with a kim wipe. Tumors were cut in half and centrifuged at 400 x g on a Nylon Mesh filter with 20wm pores (EMB catalog #NY2004700). 2-5wL of fluid was isolated from each tumor. Ammonium was immediately measured using a colorimetric assay (Abeam #ab83360).
  • Cytotoxicity Assay Cell viability was assessed using a standard Propidium Iodide and Flow Cytometry protocol (40). Briefly, cells were trypsinized, washed, re-suspended in PBS and treated with lwg/mL Propidium Iodide (Sigma). Samples were run on an LSR II Flow Cytometer (BD Biosciences) and cell populations were gated dependent on fluorescence with a 488nm laser.
  • NFb Ammonia
  • NFb in cancer has never been investigated. It was discovered NFb generated in breast cancer metabolism is efficiently recycled as a re-purposed nitrogen source for amino acid synthesis (Spinelli et al., Science, 2017, hereby incorporated by reference in its entirety). NFb recycling stimulated breast cancer proliferation, and inhibition of assimilation repressed breast cancer proliferation in vitro.
  • NFb was a dominant nitrogen source in vitro, these findings were tested in ER positive breast cancer xenograft mouse models. Tracking the fate of NFb in tumors was enabled by subcutaneous injection of 15 NFb. It was found that NFb was a nitrogen donor to amino acids via GDH in vivo ( Figure 22, Parts A-C), which is consistent with previously discussed in vitro studies.
  • Ammonia is Assimilated in Primary Breast Cancer Patients

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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

L'invention concerne des méthodes et des compositions pour le traitement du cancer ou d'une tumeur chez un sujet, comprenant l'administration au sujet d'une composition comprenant un agent qui diminue la quantité d'ammoniac chez le sujet.
PCT/US2018/022593 2017-03-15 2018-03-15 Méthodes et compositions pour le traitement du cancer WO2018170234A1 (fr)

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US4650587A (en) 1982-09-09 1987-03-17 Akzona Incorporated Ammonia scavenger
US4460555A (en) 1983-08-25 1984-07-17 Organon Teknika Corporation Ammonia scavenger
US8642012B2 (en) 2008-04-29 2014-02-04 Hyperion Therapeutics, Inc. Methods of treatment using ammonia-scavenging drugs
WO2016085887A1 (fr) * 2014-11-24 2016-06-02 Ucl Business Plc Traitement de maladies associées à l'activation des cellules hépatiques étoilées aux moyen de thérapies d'abaissement du taux d'ammoniac

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